Indium(III) bromide (CAS 13465-09-3)
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Indium(III) bromide (InBr3) is a solid compound characterized by its white crystalline structure, composed of indium and bromine atoms. This material possesses properties such as non-volatility, non-flammability, and relative stability. Indium(III) bromide finds extensive use in various scientific research applications. It acts as a catalyst in organic synthesis reactions, facilitating the formation of essential carbon-carbon bonds. Additionally, it plays a role in the synthesis of organic compounds and the preparation of specialty chemicals. Moreover, Indium(III) bromide serves as a key component in the preparation of organometallic compounds. The functionality of Indium(III) bromide resides in its role as a Lewis acid, demonstrating an ability to accept a pair of electrons from a Lewis base to establish a covalent bond. This Lewis acid-base interaction between Indium(III) bromide and the Lewis base serves as the driving force behind the progress of the reaction.
Indium(III) bromide (CAS 13465-09-3) References
- Polarographic determination of indium(III) after salting-out extraction of the bromide complex into acetonitrile. | Nagaosa, Y. 1979. Talanta. 26: 987-90. PMID: 18962561
- Oxidative Coupling of Terminal Alkynes with Aldehydes Leading to Alkynyl Ketones by Using Indium(III) Bromide. | Ogiwara, Y., et al. 2015. Chemistry. 21: 18598-600. PMID: 26507682
- Indium(III) bromide-mediated β-selective thioglycosylation of 1,2,4-O-orthoacetylglucose derivatives. | Ikuta, D., et al. 2022. Carbohydr Res. 519: 108609. PMID: 35728391
- Indium(III)/2-benzoylpyridine chemistry: interesting indium(III) bromide-assisted transformations of the ligand. | Stamou, C., et al. 2022. Dalton Trans. 51: 15771-15782. PMID: 36178466
- Indium (III) bromide catalyzed cleavage of cyclic and acyclic ethers: An efficient and practical ring opening reaction | JS Yadav, BVS Reddy, PMK Reddy, U Dash. 2007. Journal of Molecular Catalysis A: Chemical. 271: 266-269.
- Oxidative coupling of terminal alkynes with aldehydes leading to alkynyl ketones by using indium (III) bromide | Y Ogiwara, M Kubota, K Kurogi. 2015. A European Journal. 21: 18598-18600.
- Methoxyl-substituted phosphine ligand properties and a case study of formation adducts to indium (III) bromide by DFT calculations | H Yang, B Xing, J Zhao, G Ma. 2022. Polyhedron. 225: 116043.
- Indium(III) bromide-mediated β-selective thioglycosylation of 1,2,4-O-orthoacetylglucose derivatives | D Ikuta, K Kumagai, T Hagimori, T Hirokane. 108609. Carbohydrate Research. 519: 2022.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Indium(III) bromide, 10 g | sc-250152 | 10 g | $140.00 |